HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041919Generated: November 3, 2026
6-Chloro-2-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purine → N-(4-(Dipropylphosphoryl)phenyl)-2-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine
https://huagongshe.com/reaction/2041919
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Chloro-2-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 11210740 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-(Dipropylphosphoryl)aniline | HCID 59994540 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-(Dipropylphosphoryl)phenyl)-2-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine | HCID 86631259 | — |
Reaction Steps
Potassium tert-Butoxide (0.19 g, 1.65 mmol) was suspended in 4.5 mL anhydrous THF under nitrogen and cooled to −10° C. in an ice-salt bath. 4-(Dipropylphosphoryl)benzenamine (0.12 g, 0.55 mmol) was added to the suspension and the mixture was stirred at −10° C. for 30 min. 6-Chloro-2-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (Tetrahedron 2002, 58, 7911-7923, 0.18 mg, 0.5 mmol) was then added to the reaction mixture and the content was warmed to room temperature and stirred over night. The reaction mixture was cooled to 0° C., and quenched by the addition of 0.1 N HCl (˜500 mL). The mixture was concentrated on a rotavapor. The residue was partitioned between ethyl acetate (10 mL)/water (4 mL), organic layer was separated and washed with 0.1 N HCl (4×4 mL), saturated NaHCO3 (4 mL), brine (4 mL), and dried over Na2SO4. The final product was obtained by flash column chromatography on silica gel (7.5% MeOH/DCM).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586566B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-b0a2a3b6468542f38f2c2c43d5b24520 |
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| Source note | uspto-grants-2013_11 |
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